Gadoteridol • ChemWhat中文网 | 凯望化学与生物数据库

Gadoteridol Impurity 3 CAS#: 144003-28-1

By great_watson-int, 7th July 2024

Identification	Physical Data	Spectra
Route of Synthesis (ROS)	Safety and Hazards	Other Data

Identification

Physical Data

Appearance	No data available
Solubility	No data available
Flash Point	No data available
Refractive index	No data available
Sensitivity	No data available
Melting Point	No data available

Spectra

No data available

Route of Synthesis (ROS)

No data available

Safety and Hazards

No data available

Other Data

HS Code	382290
Storage	At room temperature and away from light
Related Chemicals	112193-75-6 (free base)

Use Pattern

Gadoteridol Impurity 3 is chemically 2,2′-(1,4,7,10-Tetraazacyclododecane-1,7-diyl)diacetic acid hydrochloride. Gadoteridol Impurity 3 is supplied with detailed characterization data compliant with regulatory guideline. Gadoteridol Impurity 3 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Gadoteridol. The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ChemWhat products are for analytical purpose only and not for human use.

Gadoteridol Impurity 4 CAS#: 170454-90-7

By great_watson-int, 7th July 2024

Identification	Physical Data	Spectra
Route of Synthesis (ROS)	Safety and Hazards	Other Data

Identification

Physical Data

Appearance	No data available
Solubility	No data available
Flash Point	No data available
Refractive index	No data available
Sensitivity	No data available
Melting Point	No data available

Spectra

No data available

Route of Synthesis (ROS)

No data available

Safety and Hazards

No data available

Other Data

HS Code	382290
Storage	At room temperature and away from light
Related Chemicals	2137629-28-6 (trihydrochloride salt) ; 1429316-24-4 (disulfate salt)

Use Pattern

Gadoteridol Impurity 4 is chemically 2-(1,4,7,10-Tetraazacyclododecan-1-yl)acetic acid. Gadoteridol Impurity 4 is supplied with detailed characterization data compliant with regulatory guideline. Gadoteridol Impurity 4 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Gadoteridol. The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ChemWhat products are for analytical purpose only and not for human use.

Gadoteridol Impurity 6 CAS#: N/A

By great_watson-int, 7th July 2024

Identification	Physical Data	Spectra
Route of Synthesis (ROS)	Safety and Hazards	Other Data

Identification

Physical Data

Appearance	No data available
Solubility	No data available
Flash Point	No data available
Refractive index	No data available
Sensitivity	No data available
Melting Point	No data available

Spectra

No data available

Route of Synthesis (ROS)

No data available

Safety and Hazards

No data available

Other Data

HS Code	382290
Storage	At room temperature and away from light
Related Chemicals	138884-14-7 (free base)

Use Pattern

Gadoteridol Impurity 6 is chemically Gadolinium(III) 2,2′,2”-(10-(1-hydroxypropan-2-yl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetate. Gadoteridol Impurity 6 is supplied with detailed characterization data compliant with regulatory guideline. Gadoteridol Impurity 6 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Gadoteridol. The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ChemWhat products are for analytical purpose only and not for human use.

Gadoteridol Impurity 5 CAS#: 229312-33-8

By great_watson-int, 7th July 2024

Identification	Physical Data	Spectra
Route of Synthesis (ROS)	Safety and Hazards	Other Data

Identification

Physical Data

Appearance	No data available
Solubility	No data available
Flash Point	No data available
Refractive index	No data available
Sensitivity	No data available
Melting Point	No data available

Spectra

No data available

Route of Synthesis (ROS)

No data available

Safety and Hazards

No data available

Other Data

HS Code	382290
Storage	At room temperature and away from light
Related Chemicals

Use Pattern

Gadoteridol Impurity 5 is chemically 2,2′-(13-Oxo-1,4,7,10-tetraazabicyclo[8.2.1]tridecane-4,7-diyl)diacetic acid. Gadoteridol Impurity 5 is supplied with detailed characterization data compliant with regulatory guideline. Gadoteridol Impurity 5 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Gadoteridol. The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ChemWhat products are for analytical purpose only and not for human use.

Gadoteridol Impurity 1 CAS#: 114873-37-9

By great_watson-int, 7th July 2024

Identification	Physical Data	Spectra
Route of Synthesis (ROS)	Safety and Hazards	Other Data

Identification

Physical Data

Appearance	No data available
Solubility	No data available
Flash Point	No data available
Refractive index	No data available
Sensitivity	No data available
Melting Point	No data available

Spectra

No data available

Route of Synthesis (ROS)

No data available

Safety and Hazards

No data available

Other Data

HS Code	382290
Storage	At room temperature and away from light
Related Chemicals

Use Pattern

Gadoteridol Impurity 1 is chemically 2,2’,2”-(1,4,7,10-Tetraazacyclododecane-1,4,7-triyl)triacetic acid. Gadoteridol Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Gadoteridol Impurity 1 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Gadoteridol. The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ChemWhat products are for analytical purpose only and not for human use.

Gadoteridol Nitroso Impurity 1 CAS#: 2892260-33-0

By great_watson-int, 7th July 2024

Identification	Physical Data	Spectra
Route of Synthesis (ROS)	Safety and Hazards	Other Data

Identification

Physical Data

Appearance	No data available
Solubility	No data available
Flash Point	No data available
Refractive index	No data available
Sensitivity	No data available
Melting Point	No data available

Spectra

No data available

Route of Synthesis (ROS)

No data available

Safety and Hazards

No data available

Other Data

HS Code	382290
Storage	At room temperature and away from light
Related Chemicals

Use Pattern

Gadoteridol Nitroso Impurity 1 is chemically 2,2′,2”-(10-nitroso-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetic acid. Gadoteridol Nitroso Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Gadoteridol Nitroso Impurity 1 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Gadoteridol. The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ChemWhat products are for analytical purpose only and not for human use.

Gadoteridol USP Related Compound C CAS#: 220182-19-4

By great_watson-int, 6th July 2024

Identification	Physical Data	Spectra
Route of Synthesis (ROS)	Safety and Hazards	Other Data

Identification

Physical Data

Appearance	No data available
Solubility	No data available
Flash Point	No data available
Refractive index	No data available
Sensitivity	No data available
Melting Point	No data available

Spectra

No data available

Route of Synthesis (ROS)

No data available

Safety and Hazards

No data available

Other Data

HS Code	382290
Storage	At room temperature and away from light
Related Chemicals

Use Pattern

Gadoteridol USP Related Compound C is chemically 2,2′-(11-Oxo-1,4,7,10-tetraazabicyclo[8.2.2]tetradecane-4,7-diyl)diacetic acid. Gadoteridol USP Related Compound C is supplied with detailed characterization data compliant with regulatory guideline. Gadoteridol USP Related Compound C can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Gadoteridol. The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ChemWhat products are for analytical purpose only and not for human use.

Gadoteridol CAS#: 120066-54-8

By great_watson-int, 6th July 2024

Identification	Physical Data	Spectra
Route of Synthesis (ROS)	Safety and Hazards	Other Data

Identification

Physical Data

Appearance	No data available
Solubility	No data available
Flash Point	No data available
Refractive index	No data available
Sensitivity	No data available
Melting Point	No data available

Spectra

No data available

Route of Synthesis (ROS)

No data available

Safety and Hazards

No data available

Other Data

HS Code	382290
Storage	At room temperature and away from light
Related Chemicals

Use Pattern

Gadoteridol is chemically [10-(2-Hydroxypropyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triacetato(3-)-N1,N4,N7,N10,O1,O4,O7,O10]gadolinium. Gadoteridol is supplied with detailed characterization data compliant with regulatory guideline. Gadoteridol can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Gadoteridol. The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ChemWhat products are for analytical purpose only and not for human use.

Gadoteridol Impurity 2 CAS#: 60239-18-1

By great_watson-int, 6th July 2024

Identification	Physical Data	Spectra
Route of Synthesis (ROS)	Safety and Hazards	Other Data

Identification

Physical Data

Appearance	No data available
Solubility	No data available
Flash Point	No data available
Refractive index	No data available
Sensitivity	No data available
Melting Point	No data available

Spectra

No data available

Route of Synthesis (ROS)

No data available

Safety and Hazards

No data available

Other Data

HS Code	382290
Storage	At room temperature and away from light
Related Chemicals

Use Pattern

Gadoteridol Impurity 2 is chemically 1,4,7,10-Tetraazacyclododecane-1,4,7,10-tetraacetic acid . It is also known as Tetraxetan ; DOTA. Gadoteridol Impurity 2 is supplied with detailed characterization data compliant with regulatory guideline. Gadoteridol Impurity 2 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Gadoteridol. The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ChemWhat products are for analytical purpose only and not for human use.

英文名	Gadoteridol Impurity 3
分子结构
CAS编号	144003-28-1
EINECS Number
MDL Number
Beilstein Registry Number
别名	2,2′-(1,4,7,10-Tetraazacyclododecane-1,7-diyl)diacetic acid hydrochloride
分子式	C12H24N4O4 : HCl
分子量	288.3 : 36.5
InChI
InChI Key
Canonical SMILES	OC(CN(CCNCC1)CCNCCN1CC(O)=O)=O.Cl

英文名	Gadoteridol Impurity 4
分子结构
CAS编号	170454-90-7
EINECS Number
MDL Number
Beilstein Registry Number
别名	2-(1,4,7,10-Tetraazacyclododecan-1-yl)acetic acid
分子式	C10H22N4O2
分子量	230.3
InChI
InChI Key
Canonical SMILES	O=C(O)CN1CCNCCNCCNCC1

英文名	Gadoteridol Impurity 6
分子结构
CAS编号	N/A
EINECS Number
MDL Number
Beilstein Registry Number
别名	Gadolinium(III) 2,2′,2”-(10-(1-hydroxypropan-2-yl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetate
分子式	C17H29N4O7 : Gd
分子量	401.4 : 157.3
InChI
InChI Key
Canonical SMILES

英文名	Gadoteridol Impurity 5
分子结构
CAS编号	229312-33-8
EINECS Number
MDL Number
Beilstein Registry Number
别名	2,2′-(13-Oxo-1,4,7,10-tetraazabicyclo[8.2.1]tridecane-4,7-diyl)diacetic acid
分子式	C13H22N4O5
分子量	314.3
InChI
InChI Key
Canonical SMILES	O=C1N2CCN(CC(O)=O)CCN(CC(O)=O)CCN1CC2

英文名	Gadoteridol Impurity 1
分子结构
CAS编号	114873-37-9
EINECS Number
MDL Number
Beilstein Registry Number
别名	2,2’,2”-(1,4,7,10-Tetraazacyclododecane-1,4,7-triyl)triacetic acid
分子式	C14H26N4O6
分子量	346.4
InChI
InChI Key
Canonical SMILES	O=C(O)CN1CCN(CC(O)=O)CCN(CC(O)=O)CCNCC1

英文名	Gadoteridol Nitroso Impurity 1
分子结构
CAS编号	2892260-33-0
EINECS Number
MDL Number
Beilstein Registry Number
别名	2,2′,2”-(10-nitroso-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetic acid
分子式	C14H25N5O7
分子量	375.4
InChI
InChI Key
Canonical SMILES	O=NN1CCN(CC(O)=O)CCN(CC(O)=O)CCN(CC(O)=O)CC1

英文名	Gadoteridol USP Related Compound C
分子结构
CAS编号	220182-19-4
EINECS Number
MDL Number
Beilstein Registry Number
别名	2,2′-(11-Oxo-1,4,7,10-tetraazabicyclo[8.2.2]tetradecane-4,7-diyl)diacetic acid
分子式	C14H24N4O5
分子量	328.4
InChI
InChI Key
Canonical SMILES	O=C1CN(CCN2CC(O)=O)CCN1CCN(CC2)CC(O)=O

英文名	Gadoteridol
分子结构
CAS编号	120066-54-8
EINECS Number
MDL Number
Beilstein Registry Number
别名	[10-(2-Hydroxypropyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triacetato(3-)-N1,N4,N7,N10,O1,O4,O7,O10]gadolinium
分子式	C17H29GdN4O7
分子量	558.7
InChI
InChI Key
Canonical SMILES	CC1[OH][Gd+3]([N]2(CC3)CC4=O)([N]5(CC6)CC7=O)([N]36CC8=O)([O-]8)([O-]7)([O-]4)[N](CC5)(CC2)C1

英文名	Gadoteridol Impurity 2
分子结构
CAS编号	60239-18-1
EINECS Number
MDL Number
Beilstein Registry Number
别名	1,4,7,10-Tetraazacyclododecane-1,4,7,10-tetraacetic acid
分子式	C16H28N4O8
分子量	404.4
InChI
InChI Key
Canonical SMILES	O=C(O)CN1CCN(CC(O)=O)CCN(CC(O)=O)CCN(CC(O)=O)CC1